Fanconi Anemia Type C Gene Mutation Analysis
Peripheral Myelin Protein 22 (PMP22) Gene Mutation Analysis
Trazodone, Urine
Colorado Tick Fever Virus Ab, IFA
Coagulation Factor VIII Inhibitor Screen, Plasma
Leukocyte Alkaline Phosphatase
Serine and Arginine-rich Splicing Factor 2 (SRSF2) Gene Mutation Analysis
Beta Lactoglobulin, IgG
Friedreich Ataxia Repeat Expansion, FXN (frataxin) Gene Analysis
2,3-Dinor-11Beta-Prostaglandin F2 Alpha, Urine

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/Medical Tests
/Williams Syndrome, 7q11.23 Deletion, FISH, CV

All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References

All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References

Williams Syndrome, 7q11.23 Deletion, FISH, CV
Medical Test

Clinical Utility

Access to Williams Syndrome, 7q11.23 Deletion, FISH, CV is restricted.